Product Details

SNP ID

rs201411605

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:38087208 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTCATGGGGGTCACGGGGGTCATG[G/T]GATTCACGGGCCCCTCCTCCAGAGC

Phenotype

MIM: 610409

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

BAIAP2L2 PubMed Links

Additional Information

For this assay, SNP(s) [rs3747168] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

BAIAP2L2

Gene Name

BAI1 associated protein 2 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025045.5	1601	Missense Mutation	CAC,CCC	H392P	NP_079321.3
XM_005261751.4	1601	Missense Mutation	CAC,CCC	H392P	XP_005261808.1
XM_011530379.2	1601	Missense Mutation	CAC,CCC	H392P	XP_011528681.1
XM_011530380.2	1601	Missense Mutation	CAC,CCC	H374P	XP_011528682.1
XM_011530381.2	1601	Missense Mutation	CAC,CCC	H373P	XP_011528683.1
XM_011530382.2	1601	Missense Mutation	CAC,CCC	H373P	XP_011528684.1
XM_011530383.2	1601	Missense Mutation	CAC,CCC	H368P	XP_011528685.1
XM_011530384.2	1601	Missense Mutation	CAC,CCC	H362P	XP_011528686.1
XM_011530386.2	1601	Missense Mutation	CAC,CCC	H197P	XP_011528688.1
XM_011530387.2	1601	Missense Mutation	CAC,CCC	H197P	XP_011528689.1
XM_011530388.2	1601	Missense Mutation	CAC,CCC	H185P	XP_011528690.1

Gene

SLC16A8

Gene Name

solute carrier family 16 member 8

There are no transcripts associated with this gene.

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